Trial of Effect of High-frequency Transcranial Magnetic Stimulation in the Management of Borderline Personality Disorder
Primary Purpose
Borderline Personality Disorder
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
rTMS
sham rTMS
Sponsored by
About this trial
This is an interventional treatment trial for Borderline Personality Disorder focused on measuring Borderline personality disorder, repetitive transcranial magnetic stimulation
Eligibility Criteria
Inclusion Criteria:
- Clinically diagnosed borderline personality disorder according to DSM IV.
Exclusion Criteria:
- Epilepsy
- Any metal device
- Psychotic disorders
- Bipolar mood disorder type 1
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
rTMS intervention group
Sham group
Arm Description
The rTMS intervention group undergo ten session of real TMS therapy.
Patients will undergo ten session of sham rTMS.
Outcomes
Primary Outcome Measures
Patients' reports
changes in subjective measures from baseline to tenth day of treatment
Secondary Outcome Measures
patient's report
change in subjective measures from baseline to 1 month after treatment
Patient's report
change in subjective measures form baseline to 3 month after treatment
Full Information
NCT ID
NCT01602497
First Posted
May 16, 2012
Last Updated
May 18, 2012
Sponsor
Tehran University of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT01602497
Brief Title
Trial of Effect of High-frequency Transcranial Magnetic Stimulation in the Management of Borderline Personality Disorder
Official Title
A Sham-controlled Trial of Effect of High-frequency Transcranial Magnetic Stimulation in the Management of Borderline Personality Disorder Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2012 (undefined)
Primary Completion Date
July 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tehran University of Medical Sciences
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is going to evaluate the effects of repetitive transcranial magnetic stimulation (rTMS) on Borderline Personality Disorder patients symptoms.
Detailed Description
There is a great body of literature about the positive effects of rTMS therapy on various psychiatric disorders. In this study we are going to evaluate the effects of high-frequency rTMS over the left dorsolateral prefrontal cortex (DLPFC)region in borderline personality disorder (BPD) patients. patients will be assessed by subjective measures for BPD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Borderline Personality Disorder
Keywords
Borderline personality disorder, repetitive transcranial magnetic stimulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
rTMS intervention group
Arm Type
Active Comparator
Arm Description
The rTMS intervention group undergo ten session of real TMS therapy.
Arm Title
Sham group
Arm Type
Placebo Comparator
Arm Description
Patients will undergo ten session of sham rTMS.
Intervention Type
Device
Intervention Name(s)
rTMS
Other Intervention Name(s)
repetitive transcranial magnetic stimulation
Intervention Description
Patients undergone 10 session of high-frequency rTMS therapy over their left DLPFC
Intervention Type
Device
Intervention Name(s)
sham rTMS
Other Intervention Name(s)
sham repetitive transcranial magnetic stimulation
Intervention Description
Patients will undergo ten session of sham rTMS.
Primary Outcome Measure Information:
Title
Patients' reports
Description
changes in subjective measures from baseline to tenth day of treatment
Time Frame
Change from baseline to two weeks
Secondary Outcome Measure Information:
Title
patient's report
Description
change in subjective measures from baseline to 1 month after treatment
Time Frame
Change from baseline to 1 month
Title
Patient's report
Description
change in subjective measures form baseline to 3 month after treatment
Time Frame
Change from baseline to 3 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinically diagnosed borderline personality disorder according to DSM IV.
Exclusion Criteria:
Epilepsy
Any metal device
Psychotic disorders
Bipolar mood disorder type 1
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammad Arbabi, M.D.
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Study Director
12. IPD Sharing Statement
Learn more about this trial
Trial of Effect of High-frequency Transcranial Magnetic Stimulation in the Management of Borderline Personality Disorder
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